𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Effects of dimethyl sulfide on the reaction of dibutylcopper reagents with α,β-unsaturated ketones

✍ Scribed by Celia L. Kingsbury; Kelly S. Sharp; Robin A.J. Smith


Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
623 KB
Volume
55
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.

✦ Synopsis


Addition of Me,S to a I:2 CuuBuLi mixture in toluene promotes 1,4-over I,Zaddition in reactions with a representative selection of c@-unsaturated ketones. Unlike similar reactions studied with dialkyl ethers, the effect of Me,S is not related to the amount of lithium salts in the reaction medium. The results are related to current mechanistic theories of organocuprate reactions.


📜 SIMILAR VOLUMES


ChemInform Abstract: Effects of Dimethyl
✍ Celia L. Kingsbury; Kelly S. Sharp; Robin A. J. Smith 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

A Stereoselective Synthesis of (E)-α, β-
✍ Prof. Dr. Giuseppe Bartoli; Dr. Enrico Marcantoni; Prof. Dr. Marino Petrini; Dr. 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 735 KB

## Abstract Stereoselective construction of trisubstituted alkenes has wide applicability to the synthesis of many natural products Specifically, β‐disubstituted enones are important functionalized trisubstituted alkene targets. The reaction of organocerium reagents with secondary β‐enamino ketones

Synthesis of α-iodo-α,β-unsaturated keto
✍ Asaf Alimardanov; Ei-ichi Negishi 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 262 KB

Treatment of c~-silyl-cc,[~-unsaturated enones, readily preparable as regio-and stereodefined compounds in high yields, with either 2 equiv, oflCl or one equiv, each oflC1 and A1C13 provides the corresponding cc-iodo-a,[3unsaturated enones in high yields.